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Published on: August 16, 2021
Left ventricular assist device in cardiac amyloidosis: friend or foe?
Carlotta Sciaccaluga1, Giuseppe De Carli2, Chiara Fusi2
1Department of Medical Biotechnologies, Section of Cardiology, University of Siena, Siena, Italy. carlotta.sciaccaluga@gmail.com.
Insights
Left ventricular assist devices (LVADs) offer a heart transplant alternative for advanced heart failure. This review explores LVAD challenges in cardiac amyloidosis, a condition complicating implantation and management.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Medical Technology
Background:
- Cardiac amyloidosis is an increasing cause of heart failure, often diagnosed late.
- Management of advanced heart failure in amyloid cardiomyopathy is critical.
- Left ventricular assist devices (LVADs) are an alternative to heart transplant for end-stage heart failure.
Purpose of the Study:
- To review current evidence on LVAD use in cardiac amyloidosis.
- To highlight challenges associated with LVAD implantation in this patient group.
- To discuss post-implant management considerations for LVADs in cardiac amyloidosis.
Main Methods:
- Literature review of studies on LVADs in cardiac amyloidosis.
- Analysis of anatomical and physiological challenges in LVAD implantation.
- Examination of systemic complications and management strategies post-LVAD.
Main Results:
- LVAD implantation in cardiac amyloidosis presents significant anatomical and physiological challenges.
- Systemic amyloidosis increases risks of bleeding and right ventricular failure after LVAD implant.
- Limited data exists, necessitating further research into LVAD efficacy and safety in this population.
Conclusions:
- LVADs are a potential option for advanced heart failure in cardiac amyloidosis.
- Careful patient selection and specialized management are crucial for successful outcomes.
- More research is needed to optimize LVAD therapy for cardiac amyloidosis patients.
Abstract:
The prevalence of cardiac amyloidosis has progressively increased over the last years, being recognized as a significant cause of heart failure. In fact, the management of advanced heart failure is a cornerstone treatment of amyloid cardiomyopathy due to the frequent delay in its diagnosis. Left ventricular assist devices (LVADs) have been gaining importance in the scenario of end-stage heart failure, representing an alternative to heart transplant. However, only few studies have investigated the role of LVAD in restrictive cardiomyopathies such as cardiac amyloidosis, since there are several problems to consider. In fact, both anatomical factors and the restrictive physiology of this condition make LVAD implant a relevant challenge in this subset of patients. Furthermore, due to the systemic involvement of amyloidosis, several factors have to be considered after LVAD implant, such as an increased risk of bleeding and right ventricular failure. This review attempts to summarize the current evidence of LVAD in cardiac amyloidosis, especially focusing on the challenges that this cardiomyopathy imposes both to the implant and to its management thereafter.
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